Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATACCCATCTATAAATTACCAGAG[A/G]GATCACCAACATGGCTGGGAATATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600800 | ||||||||||||||||||||
Literature Links: |
NAB1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NAB1 - NGFI-A binding protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321312.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | NP_001308241.1 | |
NM_001321313.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | NP_001308242.1 | |
NM_001321314.1 | 400 | Intron | NP_001308243.1 | |||
NM_001321315.1 | 400 | Intron | NP_001308244.1 | |||
NM_005966.3 | 400 | Intron | NP_005957.2 | |||
XM_005246582.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_005246639.1 | |
XM_005246583.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_005246640.1 | |
XM_005246586.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_005246643.1 | |
XM_005246587.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_005246644.1 | |
XM_011511219.2 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_011509521.1 | |
XM_017004170.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_016859659.1 | |
XM_017004171.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_016859660.1 | |
XM_017004172.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_016859661.1 | |
XM_017004173.1 | 400 | Intron | XP_016859662.1 | |||
XM_017004174.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_016859663.1 | |
XM_017004175.1 | 400 | Intron | XP_016859664.1 | |||
XM_017004176.1 | 400 | Missense Mutation | AGA,GGA | R,G 102 | XP_016859665.1 |